Identity
- Trade Name
- AESCULAP AICON EUDAMEDAICON FDA UDI
- Generic Name
- Device sterilization/disinfection container, reusable FDA UDI
- Device Name
- AICON container EUDAMEDAESCULAP AICON Bottom, Standard 1/1, outer length: 598 mm, outer width: 297 mm, outer heigth: 186 mm, inner length: 548 mm, inner width: 258 mm, inner heigth: 164 mm FDA UDI
- Model / Reference
- JJ130 EUDAMEDFDA UDI
- Description
- AESCULAP AICON Bottom, Standard 1/1, outer length: 598 mm, outer width: 297 mm, outer heigth: 186 mm, inner length: 548 mm, inner width: 258 mm, inner heigth: 164 mm FDA UDI
Identifiers
- Catalog Number
- JJ130 FDA UDI
- Primary DI / UDI-DI
- 04046955173792 EUDAMEDFDA UDI
- Basic UDI-DI
- 4039239000001141ZN EUDAMED
- Direct Marketing DI
- 04046955173792 EUDAMED
- FDA Product Code
- KCT FDA UDI
- EMDN Code
- S010401 TRAYS, BASKETS, TUBS FOR STERILISATION AND THEIR COMPONENTS EUDAMED
- GMDN Term
- Device sterilization/disinfection container, reusable FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 880.6850 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Aesculap Aicon by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 4039239000001141ZN | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Aesculap AG
- EUDAMED SRN
- DE-MF-000005504
Sources (2)
- EUDAMED 90433878-dcc1-49e7-9399-f7c918655112 61 fields · synced Jun 1, 2026
- FDA UDI bf1d89e6-608d-47c4-94be-4c526e6d3f4b 35 fields · synced May 30, 2026